physica pss www.pss-b.com status solidi basic solid state physics b The effects of inhomogeneous isotope distribution on the vibrational properties of isotope enriched double walled carbon nanotubes V. Zólyomi 1, 2, F. Simon 3, 4, Á. Rusznyák 2, R. Pfeiffer 3, H. Peterlik 3, H. Kuzmany 3, and J. Kürti 2 1 Research Institute for Solid State Physics and Optics of the Hungarian Academy of Sciences, P.O. Box 49, 1525 Budapest, Hungary 2 Department of Biological Physics, Eötvös University, Pázmány Péter sétány 1/A, 1117 Budapest, Hungary 3 Fakultät für Physik, Universität Wien, Strudlhofgasse 4, 1090 Wien, Austria 4 Budapest University of Technology and Economics, Institute of Physics and Condensed Matter Research Group of the Hungarian Academy of Sciences, P.O. Box 91, 1521 Budapest, Hungary Received 14 May 2007, revised 26 June 2007, accepted 26 June 2007 Published online 2 October 2007 PACS 63.22. m, 71.15.Mb, 78.30.Na, 78.67.Ch The radial breathing mode in the Raman spectrum of 13 C isotope enriched single walled carbon nanotubes is inhomogeneously broadened due to the random distribution of isotopes. We study this effect theoretically using density functional theory within the local density approximation and compare the result with experiments on isotope engineered double walled carbon nanotubes in which the inner tubes were grown from a mixture of 13 C enriched fullerenes and natural fullerenes. As explained by the calculations, this synthesis procedure leads to an increased inhomogeneity compared to a case when only enriched fullerenes are used. The good agreement between the measurements and calculations shows the absence of carbon diffusion along the tube axis during inner tube growth, and presents a strong support of the theory that inner tube growth is governed by Stone Wales transformations following the interconnection of fullerenes. phys. stat. sol. (b) 244, No. 11, 4257 4260 (2007) / DOI 10.1002/pssb.200776146 REPRINT
Original Paper phys. stat. sol. (b) 244, No. 11, 4257 4260 (2007) / DOI 10.1002/pssb.200776146 The effects of inhomogeneous isotope distribution on the vibrational properties of isotope enriched double walled carbon nanotubes V. Zólyomi *, 1, 2, F. Simon 3, 4, Á. Rusznyák 2, R. Pfeiffer 3, H. Peterlik 3, H. Kuzmany 3, and J. Kürti 2 1 Research Institute for Solid State Physics and Optics of the Hungarian Academy of Sciences, P.O. Box 49, 1525 Budapest, Hungary 2 Department of Biological Physics, Eötvös University, Pázmány Péter sétány 1/A, 1117 Budapest, Hungary 3 Fakultät für Physik, Universität Wien, Strudlhofgasse 4, 1090 Wien, Austria 4 Budapest University of Technology and Economics, Institute of Physics and Condensed Matter Research Group of the Hungarian Academy of Sciences, P.O. Box 91, 1521 Budapest, Hungary Received 14 May 2007, revised 26 June 2007, accepted 26 June 2007 Published online 2 October 2007 PACS 63.22. m, 71.15.Mb, 78.30.Na, 78.67.Ch The radial breathing mode in the Raman spectrum of 13 C isotope enriched single walled carbon nanotubes is inhomogeneously broadened due to the random distribution of isotopes. We study this effect theoretically using density functional theory within the local density approximation and compare the result with experiments on isotope engineered double walled carbon nanotubes in which the inner tubes were grown from a mixture of 13 C enriched fullerenes and natural fullerenes. As explained by the calculations, this synthesis procedure leads to an increased inhomogeneity compared to a case when only enriched fullerenes are used. The good agreement between the measurements and calculations shows the absence of carbon diffusion along the tube axis during inner tube growth, and presents a strong support of the theory that inner tube growth is governed by Stone Wales transformations following the interconnection of fullerenes. 1 Introduction Recently, we prepared isotope engineered (IEd) carbon nanotubes which allowed Raman vibrational analysis [1] and NMR studies of the tube electronic properties [2]. The IEd nanotubes were produced by annealing from 13 C enriched fullerenes (C 60, C 70,...) encapsulated inside natural carbon single walled carbon nanotube (SWCNT) host outer tubes. Open questions remain concerning the growth mechanism of inner tubes and the random distribution of 12 C and 13 C isotopes. Two mechanisms have been suggested for inner tube growth: (i) from di- or polymerized encapsulated fullerenes [3 5] through Stone Wales transformations [6], (ii) from completely disintegrated fullerenes [7]. The random isotope distribution was found to induce an inhomogeneous broadening of the Raman modes, best observed for the radial breathing mode (RBM). Results on samples that were produced by using a mixture of enriched and non-enriched fullerenes as filling material yields a larger broadening * Corresponding author: e-mail: zachary@evelyn.elte.hu, Phone: +36 1 392 2222, Fax: +36 1 392 2219
4258 V. Zólyomi et al.: Isotopic broadening effects in the RBM of DWCNTs than expected. This behavior can help to decide which of the two possible growth mechanisms is actually realized during synthesis. Here we present calculations on the isotope distribution related inhomogeneous broadening for the RBM of 13 C enriched inner tubes using density functional theory within the local density approximation on SWCNT cell sizes which are sufficient for convergence of the data [10]. We synthesized two kinds of 13 C enriched inner tubes: made from 13 C enriched fullerenes (uniform enrichment) and from mixtures of natural and 13 C enriched fullerenes (mixed enrichment). We observed that the RBMs are a factor 3 more broadened for the mixed enrichment than for the uniform enrichment at the same overall enrichment levels. The relative difference is well reproduced by the calculations if inhomogeneous clustering of 13 C rich and poor regions are assumed along the inner tubes. A scaling of the data by a factor of 1.5 2 yields quantitatively accurate agreement between theory and experiment. The results presented here prove the absence of carbon diffusion along the tube axis during inner tube growth and are a strong support of inner tube growth through Stone Wales transformations from preformed fullerene dimers or oligomers. 2 Method We used the VASP density functional theory code [8] at the LDA level and PAW method to calculate the inhomogeneous broadening of the RBM mode for three experimentally relevant SWCNTs: (10,0), (7,4), and (5,5) (the inner tube diameter range is centered around 7 Å). Long range force constants were taken into account to ensure high accuracy of the frequencies: the length of the supercells used to calculate the Hessian matrices were 12.7 Å, 13.6 Å, and 14.7 Å for (10,0), (7,4), and (5,5), respectively. In order to calculate the inhomogeneous broadening, the dynamical matrices of the tubes were constructed and diagonalized using a large number of different random distributions of 12 C and 13 C nuclei for the mass matrices. Once the RBM mode is obtained after the diagonalization, the inhomogeneous broadening is determined by calculating the standard deviation of RBM frequencies for all random isotope distributions. Two grades of 13 C enriched fullerenes were used to prepare fullerene peapods, with enrichment levels of c = 0.28 and 0.82. We synthesized two different kinds of peapod materials: the so-called uniform filling sample (where the encapsulated fullerenes were alike, i.e. from one enrichment grade) and the socalled mixed filling sample (where c = 0.28 and natural C 60 were mixed 1:1). The peapods were transformed to double walled carbon nanotubes (DWCNTs) following Ref. [9]. DWCNTs based on uniformly filled peapods with different enrichment grades are denoted as Nat C, 13 C 0.28 and 13 C 0.82 DWCNT. The DWCNT based on the fullerene mixture is denoted as 13 C 0.15 M DWCNT, reflecting its average c = 0.15 enrichment. Our calculations have shown [1] that the broadening follows a parabola-like function with a maximum at c = 0.5, suggesting that at c = 0.15 a smaller broadening is expected than at c = 0.28. However, a much larger broadening was observed for the former sample (see Ref. [10]). These findings clearly suggest the absence of carbon diffusion along the tube axis during inner tube growth and are a strong support of inner tube growth through Stone Wales transformations from interconnected fullerenes. 3 Results Using the method detailed above, we have calculated the inhomogeneous broadening of the RBM frequency of the (10,0), (7,4), and (5,5) SWCNTs. In the case of the uniform filling method, the 13 C isotopes are uniformly distributed in the supercell along the tube axis: the 13 C nuclei are randomly placed within the entire supercell, with no predefined non-enriched regions. We have calculated the inhomogeneous Gaussian broadening for 10%, 30%, 50%, 70%, and 90% 13 C content for all three tubes (see Fig. 1). As expected, in all three cases the broadening increases with increasing level of enrichment until 13 C content reaches 50%, where the broadening has a maximum. We find a slight chirality dependence, and that the calculation underestimates the experimental broadening by about a factor of 1.5 2 (the underestimation is discussed in Ref. [10]). www.pss-b.com
Original Paper phys. stat. sol. (b) 244, No. 11 (2007) 4259 Fig. 1 Calculated inhomogeneous broadening of the RBM mode of the (10,0), (7,4), and (5,5) SWCNTs (diamonds, squares, and crosses, respectively), compared with measurements (circles). All values are FWHM. The calculated results are upscaled by a factor of 1.65 [10]. The mixed filling derived tubes were studied by performing calculations at an average enrichment level of 15%, but assuming that the nanotube is composed of enriched (30%) and non-enriched (0%) sections, which follow each other randomly in 1:1 ratio using the same section size as above. The calculations are in very good qualitative agreement with the experiments: a significantly larger broadening is found than in the case of the uniform filling derived DWCNTs (see upper left corner of Fig. 1). We find no chirality dependence here, but the magnitude of the broadening is once again underestimated by a factor of 1.5 2. If all of the calculated results are upscaled by a factor of 1.65, then all calculated values for the mixed filling derived DWCNTs fall within the errorbar around the experimentally obtained value. At the same time, the theoretical results on the uniform filling derived (5,5) inner tube also match the experimental results after this same upscaling, which shows that the relative increase of the inhomogeneous broadening for this tube is in excellent agreement with the experiments. 4 Discussion: Absence of carbon diffusion The results detailed above are a clear indication that there is very little diffusion of carbon atoms along the tube axis during the creation of the inner tube in the peapod-to-dwcnt transformation process. An inner tube growth mechanism which satisfies this experimental observation was suggested in Refs. [3 5]: molecular dynamics calculations and transmission electron microscopy have shown that covalently bound fullerenes are formed as precursors; these structures can proceed toward short inner tube sections with low energy Stone Wales transformations. This mechanism ensures that carbons do not diffuse along the tube axis, thus our results are a strong support for this kind of growth mechanism. Alternative models considered the inner tube growth from completely disintegrated fullerenes into e.g. C 2 units [7]. However, in this model strong carbon diffusion along the tube axis would be expected. In contrast, our results show that there is practically no diffusion, which suggests that the growth of the inner tube does not occur by a complete disintegration of the fullerenes, but rather by a Stone Wales type fusion mechanism. 5 Conclusions We have performed first principles calculations on the inhomogeneous broadening of the Raman RBM lines of isotope engineered double walled carbon nanotubes, and compared the calculations to our ex- www.pss-b.com
4260 V. Zólyomi et al.: Isotopic broadening effects in the RBM of DWCNTs perimental results. We have shown that the broadening grows monotonically with increasing enrichment, peaks at 50% 13 C content, then decreases monotonically and drops back to 0 at 100% 13 C content. We have found experimentally that if the filling of the peapod is performed with a mixture of enriched and non-enriched fullerenes, the Raman spectra of the resulting inner tubes show a much larger broadening than in the case of the uniform filling method. Our calculations have shown that this finding is consistent with the assumption that the local enrichment level of the double walled tube reflects the local enrichment level of the corresponding peapod material. The good agreement between our calculations and experiments clearly indicates that there is very little diffusion of carbon atoms along the tube axis, supporting the theory that the inner tubes are formed by Stone Wales transformations from interconnected fullerenes. Acknowledgements Work supported by OTKA Grants No. F68852, K60576, TS049881, F61733 and NK60984 in Hungary. F.S. acknowledges the Zoltán Magyary postdoctoral fellowship and V.Z. the Bolyai fellowship of the Hungarian Academy of Sciences. References [1] F. Simon, C. Kramberger, R. Pfeiffer, H. Kuzmany, V. Zólyomi, J. Kürti, P. M. Singer, and H. Alloul, Phys. Rev. Lett. 95, 017401 (2005). [2] P. M. Singer, P. Wzietek, H. Alloul, F. Simon, and H. Kuzmany, Phys. Rev. Lett. 95, 236403 (2005). [3] Y. Zhao, B. I. Yakobson, and R. E. Smalley, Phys. Rev. Lett. 88, 185501 (2002). [4] S. W. Han, M. Yoon, S. Berber, N. Park, E. Osawa, J. Ihm, and D. Tománek, Phys. Rev. B 70, 113402 (2004). [5] S. Bandow, T. Hiraoka, T. Yumura, K. Hirahara, H. Shinohara, and S. Iijima, Chem. Phys. Lett. 384, 320 (2004). [6] A. J. Stone and D. J. Wales, Chem. Phys. Lett. 128, 501 (1986). [7] F. Simon, A. Kukovecz, C. Kramberger, R. Pfeiffer, F. Hasi, H. Kuzmany, and H. Kataura, Phys. Rev. B 71, 165439 (2005). [8] G. Kresse and J. Hafner, Phys. Rev. B 48, 13115 (1993). [9] S. Bandow, M. Takizawa, K. Hirahara, M. Yudasaka, and S. Iijima, Chem. Phys. Lett. 337, 48 (2001). [10] V. Zólyomi, F. Simon, Á. Rusznyák, R. Pfeiffer, H. Peterlik, H. Kuzmany, and J. Kürti, Phys. Rev. B 75, 195419 (2007). www.pss-b.com